Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:2690

Neutropenia-monocytopenia-deafness syndrome

Also called Neutropenia-monocytopenia-hearing loss syndrome

Body system
Immunological diseases
Inheritance pattern
Unknown
Typical age of onset
Infancy, Neonatal
Estimated prevalence
<1 / 1 000 000 (Worldwide)
Rarity class
<1 / 1 000 000

ORPHA:2690 is classified under "Immunological diseases" in the Orphanet nomenclature.

Common signs

  • Sensorineural hearing impairment
  • Abnormality of neutrophils
  • Abnormal macrophage morphology
  • Abnormality of immune system physiology